Entity Details

Primary name TIA1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP31483
EntryNameTIA1_HUMAN
FullNameNucleolysin TIA-1 isoform p40
TaxID9606
Evidenceevidence at protein level
Length386
SequenceStatuscomplete
DateCreated1993-07-01
DateModified2021-06-02

Ontological Relatives

GenesTIA1

GO terms

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GOName
GO:0001818 negative regulation of cytokine production
GO:0003723 RNA binding
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0006915 apoptotic process
GO:0008143 poly(A) binding
GO:0008543 fibroblast growth factor receptor signaling pathway
GO:0010494 cytoplasmic stress granule
GO:0017148 negative regulation of translation
GO:0035925 mRNA 3'-UTR AU-rich region binding
GO:0048024 regulation of mRNA splicing, via spliceosome
GO:0097165 nuclear stress granule
GO:1903608 protein localization to cytoplasmic stress granule
GO:1904037 positive regulation of epithelial cell apoptotic process
GO:1990904 ribonucleoprotein complex

Subcellular Location

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Subcellular Location
Cytoplasm
Nucleus

Domains

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DomainNameCategoryType
IPR000504 RNA recognition motif domainDomainDomain
IPR003954 RNA recognition motif domain, eukaryoteDomainDomain
IPR012677 Nucleotide-binding alpha-beta plait domain superfamilyFamilyHomologous superfamily
IPR034830 TIA-1, RNA recognition motif 2DomainDomain
IPR034832 TIA-1, RNA recognition motif 3DomainDomain
IPR035979 RNA-binding domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
604454 OMIMWelander distal myopathy (WDM)An autosomal dominant disorder characterized by adult onset of distal muscle weakness predominantly affecting the distal long extensors of the hands, with slow progression to involve all small hand muscles and the lower legs. Skeletal muscle biopsy shows myopathic changes and prominent rimmed vacuoles. Rare homozygous patients showed earlier onset, faster progression, and proximal muscle involvement. The disease is caused by variants affecting the gene represented in this entry.

Interactions

43 interactions

InteractorPartnerSourcesPublicationsLink
TIA1_HUMANWBP4_HUMANBioGRID, IntAct28838205 details
TIA1_HUMANRU1C_HUMANIntAct12486009 details
TIA1_HUMANFASTK_HUMANBioGRID, HPRD7544399 details
TIA1_HUMANTAU_HUMANBioGRID27160897 27460788 details
TIA1_HUMANTOB1_HUMANUniProt18377426 details
TIA1_HUMANRC3H2_HUMANBioGRID, MINT20412057 29395067 details
TIA1_HUMANDCP1A_HUMANHPIDb, MINT20412057 24965446 details
TIA1_HUMANSND1_HUMANMINT20643132 details
TIA1_HUMANHABP4_HUMANMINT21771594 details
TIA1_HUMANDDX3X_HUMANUniProt18596238 details
TIA1_HUMANPAIRB_HUMANMINT24205981 details
TIA1_HUMANSF01_HUMANIntAct26420826 details
TIA1_HUMANYBOX1_HUMANHPIDb24965446 details
TIA1_HUMANSNRPA_HUMANIntAct12486009 details
TIA1_HUMANRU17_HUMANIntAct12486009 details
TIA1_HUMANPARK7_HUMANMINT29675578 details
TIA1_HUMANRICTR_HUMANBioGRID17461779 details
TIA1_HUMANSRSF3_HUMANBioGRID22939629 27381497 details
TIA1_HUMANWDR6_HUMANBioGRID19910486 details
TIA1_HUMANUBQL2_HUMANBioGRID30442662 details
TIA1_HUMANANXA7_HUMANBioGRID25461769 details
TIA1_HUMANTRI25_HUMANBioGRID31710640 details
TIA1_HUMAN4ET_HUMANBioGRID29395067 details
TIA1_HUMANFUBP3_HUMANBioGRID29395067 details
TIA1_HUMANRAVR1_HUMANBioGRID29395067 details
TIA1_HUMANSMN_HUMANBioGRID29395067 details
TIA1_HUMANTDRD3_HUMANBioGRID29395067 details
TIA1_HUMANUBP11_HUMANBioGRID29395067 details
TIA1_HUMANDDX20_HUMANBioGRID29395067 details
TIA1_HUMANGORS2_HUMANBioGRID29395067 details
TIA1_HUMANRBM20_HUMANBioGRID29395067 details
TIA1_HUMANTOP3B_HUMANBioGRID29395067 details
TIA1_HUMANTXNL1_HUMANBioGRID29395067 details
TIA1_HUMANRENT1_HUMANBioGRID29395067 details
TIA1_HUMANGEMI4_HUMANBioGRID29395067 details
TIA1_HUMANR3HD1_HUMANBioGRID29395067 details
TIA1_HUMANALG13_HUMANBioGRID29395067 details
TIA1_HUMANKCD12_HUMANBioGRID29395067 details
TIA1_HUMANMOONR_HUMANBioGRID29395067 details
TIA1_HUMANKDIS_HUMANBioGRID29395067 details
TIA1_HUMANOTUD4_HUMANBioGRID29395067 details
TIA1_HUMANRBM33_HUMANBioGRID29395067 details
TIA1_HUMANWDCP_HUMANBioGRID29395067 details